HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75106Generated: October 30, 2026
Trifluoroacetic acid → HCID 24697849, compound
https://huagongshe.com/reaction/75106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 4-(5-(trifluoromethyl)pyridin-2-ylamino)piperidine-1-carboxylate | HCID 58576452 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24697849 | HCID 24697849 | — |
Reaction Steps
0.860 g (2.49 mmol) of tert-butyl 4-(5-(trifluoromethyl)(pyridin-2-ylamino)piperidine-1-carboxylate obtained in stage 6.1. is dissolved in 8.5 ml of dichloromethane. 1.91 ml of trifluoroacetic acid are added and the mixture is stirred at ambient temperature for 4 hours. The dichloromethane is evaporated and then the residue is coevaporated twice with 10 ml of 1,2-dichloroethane. The residue is taken up in a mixture of 50 ml of ethyl acetate, 10 ml of a 1N aqueous sodium hydroxide solution and 5 ml of a 33% aqueous ammonia solution. The organic phase is separated by settling. It is washed with 2 times 10 ml of water and then with 10 ml of a saturated aqueous sodium chloride solution. It is dried over sodium sulphate and evaporated to dryness to produce 0.572 g (2.33 mmol) of product in the form of an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835418B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-99172d101c6d48db8f262eca04c25702 |
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| Source note | uspto-grants-2014_09 |
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